共 50 条
- [21] Breast cancer risk associated with missense variants in BRCA2JOURNAL OF CLINICAL ONCOLOGY, 2023, 41 (16)Yadav, SiddharthaRichardson, MarcyKaram, RachidBoddicker, Nicholas J.Hu, ChunlingTecleab, Yohannes A.Kraft, PeterWeitzel, Jeffrey N.Domchek, Susan M.Nathanson, KatherineCouch, Fergus
- [22] Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancerNature Genetics, 2014, 46 : 736 - 741Yufei WangJames D McKayThorunn RafnarZhaoming WangMaria N TimofeevaPeter BroderickXuchen ZongMarina LaplanaYongyue WeiYounghun HanAmy LloydManon Delahaye-SourdeixDaniel ChubbValerie GaborieauWilliam WheelerNilanjan ChatterjeeGudmar ThorleifssonPatrick SulemGeoffrey LiuRudolf KaaksMarc HenrionBen KinnersleyMaxime ValléeFlorence Le Calvez-KelmVictoria L StevensSusan M GapsturWei V ChenDavid ZaridzeNeonilia Szeszenia-DabrowskaJolanta LissowskaPeter RudnaiEleonora FabianovaDana MatesVladimir BenckoLenka ForetovaVladimir JanoutHans E KrokanMaiken Elvestad GabrielsenFrank SkorpenLars VattenInger NjølstadChu ChenGary GoodmanSimone BenhamouTonu VooderKristjan VälkMari NelisAndres MetspaluMarcin LenerJan Lubiński
- [23] Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancerNATURE GENETICS, 2014, 46 (07) : 736 - 741Wang, YufeiMckay, James D.Rafnar, ThorunnWang, ZhaomingTimofeeva, Maria N.Broderick, PeterZong, XuchenLaplana, MarinaWei, YongyueHan, YounghunLloyd, AmyDelahaye-Sourdeix, ManonChubb, DanielGaborieau, ValerieWheeler, WilliamChatterjee, NilanjanThorleifsson, GudmarSulem, PatrickLiu, GeoffreyKaaks, RudolfHenrion, MarcKinnersley, BenVallee, MaximeLeCalvez-Kelm, FlorenceStevens, Victoria L.Gapstur, Susan M.Chen, Wei V.Zaridze, DavidSzeszenia-Dabrowska, NeoniliaLissowska, JolantaRudnai, PeterFabianova, EleonoraMates, DanaBencko, VladimirForetova, LenkaJanout, VladimirKrokan, Hans E.Gabrielsen, Maiken ElvestadSkorpen, FrankVatten, LarsNjolstad, IngerChen, ChuGoodman, GaryBenhamou, SimoneVooder, TonuValk, KristjanNelis, MariMetspalu, AndresLener, MarcinLubinski, Jan
- [25] Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemiaBLOOD, 2004, 103 (08) : 3226 - 3229Wagner, JETolar, JLevran, OScholl, TDeffenbaugh, ASatagopan, JBen-Porat, LMah, KBatish, SDKutler, DIMacMillan, MLHanenberg, HAuerbach, AD
- [26] Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort studyJOURNAL OF HEMATOLOGY & ONCOLOGY, 2024, 17 (01)Kastellan, SvenjaKalb, ReinhardSajjad, BiaMcreynolds, Lisa J.Giri, NeelamSamuel, DavidMilde, TillElbracht, MiriamHolzhauer, SusanneNiewisch, Marena R.Kratz, Christian P.
- [27] A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assayBLOOD, 2011, 118 (09) : 2430 - 2442Biswas, KajalDas, RanabirAlter, Blanche P.Kuznetsov, Sergey G.Stauffer, StaceyNorth, Susan L.Burkett, SandraBrody, Lawrence C.Meyer, StefanByrd, R. AndrewSharan, Shyam K.
- [28] A Case of Triple-Negative Breast Cancer with Germline Pathogenic Variants in Both BRCA1 and BRCA2CASE REPORTS IN ONCOLOGY, 2021, 14 (03): : 1645 - 1651Kitahara, MiyukiHozumi, YasuoMachinaga, MitsukiHayashi, Yuka
- [29] Fanconi anemia is associated with a defect in the BRCA2 partner PALB2NATURE GENETICS, 2007, 39 (02) : 159 - 161Xia, BingDorsman, Josephine C.Ameziane, Najimde Vries, YneRooimans, Martin A.Sheng, QingPals, GerardErrami, AbdellatifGluckman, ElianeLlera, JulianWang, WeidongLivingston, David M.Joenje, Hansde Winter, Johan P.
- [30] Fanconi anemia is associated with a defect in the BRCA2 partner PALB2Nature Genetics, 2007, 39 : 159 - 161Bing XiaJosephine C DorsmanNajim AmezianeYne de VriesMartin A RooimansQing ShengGerard PalsAbdellatif ErramiEliane GluckmanJulian LleraWeidong WangDavid M LivingstonHans JoenjeJohan P de Winter